Come join my team at St. Jude Research and uncover the secrets of reversible covalent inhibitors. #Chemistry #ChemPostdocBot postdoc-stjude.icims.com/jobs/10428/job…

I'm hiring! Come join us in sunny (and not at all hellaciously hot) Merced! If you're interested in a postdoc in synthetic chemistry, focused on projects related to organometallic catalysis, then please apply! #chempostdoc aprecruit.ucmerced.edu/JPF01412

It's great to see this out in J Org Chem/Org Lett! This was a fun and interesting project to work on, many thanks to Andrew Smith James Taylor and Stefania F. Musolino for all their hard work. Best sabbatical ever St Andrews School of Chemistry!

Great story, thanks for sharing!!!

Mind-blowing work from Carl Mansson & Noah Burns out today in JACS — aqueous CuSO4 catalyzes light-promoted [2+2] Kochi–Salomon cycloaddition of simple olefins. The response from everyone I've shown this to is the same: disbelief, then delight. pubs.acs.org/doi/10.1021/ja…

What a great resource! Thanks IOCB Prague!

While there are lots of options to beat water with H-bond acceptors, for H-bond donors its not so easy. Here's a analysis of the nice dataset in Schwöbel et al. You can see that CH-donors essentially never beat water. In the NH donor class, amides usually beat water but 1/4

compound 25 - Merck | drughunters.com/3Xj1hD0 This case study of- lead optimization incorporates a “bow-tie” spirocyclopropyl group and a flipped indazole as a non-classical C-H hinge binder to improve PK properties in targeting LRRK2 for Parkinson’s disease.

Hey PUI researchers, do you qualify to publish in J Org Chem/Org Lett with free open access? If your institution has the All ACS Package and you are the submitting corresponding author, yes you do. Learn more here acsopenscience.org/customers/acs-…. We look forward to your next submission.

#ChemTwitter, the #GrenningLab is actively recruiting a postdoc! Gain mentoring experience with an amazing group of Grad/UG students! Help develop enantioselective, "energetically challenging" Cope rearrangements! Enjoy the vibrant #CollegeTownLife in Sunny Visit Gainesville, Alachua FL! #PlzRT!!

Iterating on sulfur fluoride exchange, K. Barry Sharpless and John E. Moses have introduced phosphorus fluoride exchange for building complex products from a central phosphorus hub. ‘Just one step to the left and the world is different,’ says Sharpless. chemistryworld.com/news/introduci…

Congratulations to Brittany and team! Great job! 🎉

German photographer Herlinde Koelbl asked past Nobel laureates to draw the essence of their award-winning research on the palm of their hand. Thank you, Frances Arnold, for talking to me about being one of her subjects. On Forbes --> forbes.com/sites/leslieka…

IT'S FINALLY HERE! Starting October 28th, the Synthesis Workshop Advanced Organic Chemistry course will begin releases through our regular YouTube channel for FREE, thanks to the massive efforts of presenters from many researchers from academia and industry! Support by sharing!

Fantastic resource, thank you!

Chemical Shock Wave 🌋

Spin-matched reactions 🌪 #RealTimeChem

Looking for your first step towards an independent career? We offer a 3-year-independent fellowship to support postdoc researchers from backgrounds under-represented in chemistry (e.g., women, minority ethnic, LGBTQI+, disabled, low-income backgrounds) shorturl.at/RBBpV

A postdoctoral position, funded by the The Leverhulme Trust for up to 36 months, is available to join my group Chemistry Edinburgh . The project focuses on biomimetic approaches to natural product synthesis. Deadline: 18th April 2025. elxw.fa.em3.oraclecloud.com/hcmUI/Candidat…

A postdoctoral position, funded by the The Leverhulme Trust for up to 36 months, is available to join my group Chemistry Edinburgh. The project focuses on biomimetic approaches to natural product synthesis. Deadline: 28th August 2025. elxw.fa.em3.oraclecloud.com/hcmUI/Candidat…